Shenzhen Dazhou Medical Technology Co., Ltd.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 2
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K241186 | Synthetic Bone Graft Particulate | February 21, 2025 |
| K241073 | DZ-Tabone Intervertebral Body Fusion Device | December 6, 2024 |